US4960764A - Oil-in-water-in-silicone emulsion compositions - Google Patents

Oil-in-water-in-silicone emulsion compositions Download PDF

Info

Publication number
US4960764A
US4960764A US07/312,347 US31234789A US4960764A US 4960764 A US4960764 A US 4960764A US 31234789 A US31234789 A US 31234789A US 4960764 A US4960764 A US 4960764A
Authority
US
United States
Prior art keywords
oil
phase
emulsion
water
composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US07/312,347
Inventor
Ramon Figueroa, Jr.
Bobby G. Harrison, Jr.
James P. SaNogueira
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Richardson Vicks Inc
Original Assignee
Richardson Vicks Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Richardson Vicks Inc filed Critical Richardson Vicks Inc
Priority to US07/312,347 priority Critical patent/US4960764A/en
Assigned to RICHARDSON-VICKS INC., TEN WESTPORT ROAD, WILTON, CONNECTICUT A CORP. OF DE reassignment RICHARDSON-VICKS INC., TEN WESTPORT ROAD, WILTON, CONNECTICUT A CORP. OF DE ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: FIGUEROA, RAMON JR., HARRISON, BOBBY G., SA NOGUEIRA, JAMES P.
Application granted granted Critical
Publication of US4960764A publication Critical patent/US4960764A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/06Emulsions
    • A61K8/062Oil-in-water emulsions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/06Emulsions
    • A61K8/066Multiple emulsions, e.g. water-in-oil-in-water
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/58Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
    • A61K8/585Organosilicon compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/891Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • A61K8/894Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a polyoxyalkylene group, e.g. cetyl dimethicone copolyol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/04Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations

Definitions

  • the multiphase emulsion composition is in the form of an oil phase/water phase/silicone fluid phase ("o/w/s multiple emulsion").
  • o/w/s multiple emulsion oil phase/water phase/silicone fluid phase
  • the subject o/w/s multiple emulsion may be used as a base form for various products requiring an emulsified dispersion system such as cosmetic and topical drug formulations.
  • Single emulsion skin care preparations such as lotions and creams, of the oil-in-water (o/w) type and water-in-oil (w/o) type are well known in the cosmetic art and are in daily use by consumers, the o/w type being more commonly utilized.
  • Multiphase (i.e., double) emulsion compositions such as the water-in-oil-in-water (w/o/w) type, for example see U.S. Pat. No. 4,254,105, and the oil-in-water-in oil (o/w/o) type, are of lesser commercial significance to date in the cosmetic field.
  • such single or multiphase emulsions contain water, emollients and emulsifiers as essential ingredients and cosmetically acceptable optional additives such as preservatives, antioxidants, skin conditioners, humectants, thickeners, cleansers, colorants, odorants and other components generally utilized in the cosmetic art.
  • This double emulsion composition is a dispersion of an aqueous emulsion of a finely divided (0.1-5 microns) wax material in a continuous phase made up of a small amount of an organopolysiloxane of prescribed viscosity in a large volume of a hydrocarbon solvent of prescribed aniline point and distillation range characteristics (see column 6, lines 19 et seq).
  • the particulate wax/ water emulsion is dispersed in the organopolisiloxane/hydrocarbon solvent phase by means of a non-silicone type of water-in-oil emulsifier (see column 7, lines 14 et seq).
  • Such wax polishing emulsions however, have obvious disadvantages for cosmetic usage.
  • the hydrocarbon solvent is contraindicated for skin applications due to its inherent skin-drying characteristic, indeed skin-damaging upon prolonged contact.
  • the polishing waxes are inherently water resistant and form non-permeable films, which characteristics, although suitable for application to hard surfaces such as wood or metal, are undesirable in skin care compositions.
  • a skin moisturizing multiphase emulsion composition wherein the continuous phase consists essentially of a silicone fluid component and, in addition, an effective dispersing amount of a particular silicone fluid, namely, dimethicone copolyol, is used to disperse in said continuous phase an oil-in-water (o/w) emulsion as the aqueous discontinuous phase, the oil phase of said o/w emulsion being a liquid non-particulate containing material.
  • o/w oil-in-water
  • an oil-in-water-in silicone fluid (o/w/s) emulsion composition comprising three essential components, namely, a silicone fluid component as the continuous phase, an oil-in-water (o/w) emulsion as the discontinuous phase, and dimethicone copolyol as the dispersing agent, said three components being present in the indicated approximate relative percent by weight proportions:
  • the silicone fluid continuous phase in the subject multiphase emulsion composition consists essentially of at least one liquid organopolysiloxane such as, for example, a volatile silicone fluid, for example, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, dodecamethylcyclohexasiloxane, hexamethyldisiloxane and the like, and a non-volatile silicone fluid such as, for example, dimethicone copolyol, dimethylpolysiloxane, diethylpolysiloxane, mixed C 1 -C 3 alkyl (e.g., methylethyl) polysiloxane, phenyl dimethicone and high molecular weight dimethicones (average molecular weight from about 200,000 to about 1,000,000 and, preferably, from about 300,000 to about 600,000) which may have various end-terminating groups such as hydroxy, lower C 1-3
  • the silicone fluid continuous phase consists essentially of one or more volatile silicone fluids, preferably cyclomethicone, in admixture with one or more non- volatile silicone fluids in a respective weight ratio (volatile : non-volatile) of from about 5:1 to about 25:1 and, most preferably, from about 10:1 to about 20:1.
  • volatile is meant to include liquid lower molecular weight organopolysiloxanes having a viscosity of from about 0.65 to about 5 centistokes at 25° C.; and "nonvolatile” meaning higher molecular weight liquid organopolysiloxanes having a viscosity higher than 5.
  • Liquid organopolysiloxane also known as silicone fluids
  • silicone fluids are well known and available from various commercial suppliers.
  • several such silicone fluids are distributed by the Dow Corning Corporation, Midland, Mich., under the following designations: DC 344 Fluid, the volatile cyclomethicone; DC 3225C Fluid, a 90:10 w/w mixture of cyclomethicone and dimethicone copolyol; DC X2-1401 Fluid, a 13:87 w/w mixture of dimethiconol (hydroxy- terminated dimethicone) and cyclomethicone; and DC 556 Fluid, the non-volatile phenyl dimethicone; by The General Electric Company, Silicone Products Division, Waterford, N.Y., under its "SF" designation, for example, SF-96 for dimethicone; and SF-1173 for cyclomethicone; and by Union Carbide Corporation under its "Silicone L” series, for example, Silicone L-45 for
  • the silicone fluid continuous phase is employed in amounts ranging from about 15 to about 70 percent and, preferably, from about 18 to about 40 percent, by weight of the subject o/w/s multiple emulsion.
  • dimethicone copolyol constitutes the major or total part of the silicone fluid continuous phase, it also acts as the dispersing agent for the o/w emulsion discontinuous phase.
  • the discontinuous phase in the subject o/w/s multiple emulsion composition comprises an oil-in-water emulsion of a cosmetically acceptable oily liquid phase dispersed in an aqueous phase, generally with a pH range of about 4-8.
  • the o/w emulsion contains from about 70 to about 99 percent and, preferably, from about 85 to about 95 percent, by weight of an aqueous continuous phase, from about 0.5 to about 25 percent and, preferably, from about 2 to about 18 percent, by weight of an oil discontinuous phase, and from about 0.5 to about 5 percent and, preferably, from about 1 to about 2 percent, by weight of a suitable oil-in-water emulsifier.
  • the aqueous continuous phase of the o/w emulsion may be simply water or water containing one or more soluble or dispersible cosmetically acceptable ingredients.
  • Typical such ingredients include, for example, an emulsifier with a hyprophile-lipophile balance (HLB) value from about 12 to about 20 or even higher such as sodium alkyl polyether sulfonate, polysorbate 20, polysorbate 80, polyoxyethylene 23 lauryl ether, oleth-20 and the like; a humectant such as glycerin, polyethylene glycol, pantethine and the like; a thickener such as an acrylic acid polymer denoted by the Cosmetic, Toiletry & Fragrance Association (CTFA) name "Carbomer", a natural or synthetic gum, a cellulosic derivative and the like; a preservative or antioxidant such as methyl or propyl paraben, butylated hydroxytoluene, butylated hydroxyanisole and the like
  • the oil discontinuous phase of the o/w emulsion may be simply a cosmetically acceptable oil or such oil containing one or more soluble or miscible additives generally used in cosmetic compositions.
  • Typical such oils also known as emollients, include mineral oil (heavy preferred), squalane, a vegetable oil such as sesame oil, safflower oil, castor oil, avocado oil and the like liquid non-wax oils.
  • Typical oil-soluble or oil-miscible additives include, for example, a fatty (C 12 -C 18 preferred) acid, alcohol or ester such as myristic acid, palmitic acid, lauric acid, stearic acid, cetyl alcohol, stearyl alcohol, cetyl palmitate, octyl hydroxystearate and the like, a sterol such as cholesterol and other sterol derivatives; and a natural or synthetic wax such as beeswax, spermacetti and the like; skin penetration enhancers such as C 8 -C 10 triglycerides; and such other additives as oil soluble vitamins, antioxidants, preservatives, auxilliary emulsifiers and the like.
  • a fatty (C 12 -C 18 preferred) acid, alcohol or ester such as myristic acid, palmitic acid, lauric acid, stearic acid, cetyl alcohol, stearyl alcohol, cetyl palmitate, octyl
  • the oil discontinuous phase which may contain from about 0.5 to about 10 percent by weight of such optional additives, is prepared such that it is void of particulate matter.
  • the optional wax additive very small amounts are utilized in relation to the higher amount of solubilizing oil so that no particulate wax material is present in the oil phase.
  • a particularly preferred embodiment of the oil phase comprises heavy mineral oil (0.885-0.895 specific gravity at 25° C.), cholesterol and cetyl palmitate in a respective weight ratio of about 10:5:1.
  • the oil-in-water emulsion is readily prepared by first thoroughly combining all the water-phase components and all the oil-phase components, including the essential emulsifying agent or agents, in separate vessels at elevated temperatures of about 60°-90° C. In general, the heated oil phase is then slowly added to the heated water phase using moderate to high speed mechanical dispersing means until a uniform o/w emulsion is obtained.
  • the oil-in-water emulsion it is of an appropriate emulsifier which may be in the water and/or oil phase. It is of course understood that blends of emulsifiers of varying HLB values can be used to obtain the desired HLB value as determinable in the manner described in "The Atlas HLB System” (4th printing) copyright 1963 by Atlas Chemical Industries, Inc., Wilmington, Del.
  • the emulsifier should have a hydrophile-lipophile balance such that the oil component is dispersed in the aqueous medium, generally an HLB value of not more than 14 and, preferably, from about 4 to about 12.
  • Typical emulsifiers are such nonionic and anionic surfactants as polyoxyethylene 20 sorbitan trioleate (Polysorbate 85), sorbitan monolaurate, polyoxyethylene 4 lauryl ether sodium stearate and the like.
  • the multiphase oil-in-water-in-silicone fluid (o/w/s) emulsion compositions of this invention are readily prepared by using art-recognized principles and methodologies in mixing the ingredients together and in choosing the type of mixing or dispersing equipment to be used.
  • the following Examples provide a general listing of both essential and optional components and illustrate procedures for making the subject compositions.
  • an effective dispersing amount of dimethicone copolyol is dissolved in the silicone fluid component and then the separately prepared oil-in-water emulsion is added and dispersed, for example, by mechanical dispersing means, into the silicone fluid phase at room temperature to obtain a homogeneous dispersion of the o/w emulsion therein.
  • the dimethicone copolyol dispersant maintains the o/w emulsion as the dispersed phase, also known as the discontinuous phase, in the silicone fluid continuous phase. Stable o/w/s emulsions having various dispersed phase volumes are easily and consistently prepared with high reproducibility.
  • dimethicone copolyol may also constitute all or part of the silicone fluid continuous phase component of the o/w/s multiple emulsion composition and may act both as the silicone fluid and the dispersant essential components of this invention.
  • the percentage of the essential components, the amounts and types of optional additives, and the shearing effect obtained from the mixing speed and time the o/w/s multiple emulsion can be obtained in varying viscosity ranges from lotion to heavy cream form.
  • the subject o/w/s multiple emulsion is effective as a skin care cosmetic composition, in that it provides beneficial moisturizing activity when applied to human skin, particularly to skin cosmetically characterized as dry skin, chapped skin or rough skin.
  • cosmetics such as lotions and creams which, in addition to providing said moisturizing action to the skin, may also provide other cosmetically desirable properties by incorporation of one or more skin care ingredients possessing a particular cosmetic characteristic, for example, sunscreening or sunblocking agents (a preferred embodiment), skin conditioners, cosmetic pigments and the like.
  • each of the oil and water phases of the o/w emulsion may contain optional cosmetic additives.
  • the silicone fluid component may also be utilized as a carrier of optional silicone miscible cosmetically acceptable additives.
  • Typical of such additives are silicone treated pigments and talcs; ultraviolet (U.V.) absorbers for sunscreening or sunblocking protection such as octyl methoxycinnamate, benzophenone-3, silicone treated titanium dioxide and the like; polymeric skin conditioners such as, for example, the commercially available Dow Corning® QF1-593A Fluid, a mixture of dimethyl and trimethyl polysiloxane (Dow Corning Corporation, Midland, Mich.), solubilizers for U.V. absorbers or fragrances such as, for example, C.sub. 12-C 15 alcohol benzoates; and the like.
  • U.V. absorbers for sunscreening or sunblocking protection
  • polymeric skin conditioners such as, for example, the commercially available Dow Corning® QF1-593A Fluid, a mixture of dimethyl and trimethyl polysiloxane (Dow Corning Corporation, Midland, Mich.), so
  • the subject o/w/s multiple emulsion may also be used as an effective carrier for various medicaments and drugs intended for topical skin application.
  • water soluble drugs may be incorporated into the aqueous phase of the o/w emulsion
  • oil soluble or oil miscible drugs may be incorporated into the oil phase of the o/w emulsion
  • silicone treated or silicone miscible drugs may be incorporated into the silicone fluid component.
  • An o/w emulsion is prepared from the following ingredients, identified by chemical or CTFA name. The indicated % w/w is based on the total weight of the finally prepared o/w/s multiple emulsion.
  • a suitable mechanical stirrer (Tekmar Model RW-20 stirring motor, manufactured by IKA-WERK, Germany)
  • the water and sulfonate emulsifier are heated to about 72°-75° C. and mixed. Stirring is increased until a vortex forms in the aqueous solution.
  • the thickener, Carbomer 940 is slowly added to the vortex and allowed to mix until completely hydrated and the resultant gel solution is free of gelatinous particles and is uniform in composition.
  • the temperature is maintained at about 72°-75° C. with constant agitation.
  • the oil phase ingredients are added to a separate suitably sized vessel and heated to about 80°-85° C. using slow mechanical stirring once the oil phase becomes molten. When molten, agitation is maintained to keep the oil phase unform during heating.
  • the heated oil phase is then slowly added to the heated water phase with stirring to form the o/w emulsion.
  • the mechanical dispersing means is slowed to avoid unnecessary aeration of the emulsion and mixing is continued for approximately fifteen minutes at 70°-75° C.
  • the emulsion is then cooled to about 60° C. with moderate agitation.
  • the base, triethanolamine is then slowly added to neutralize the acidic Carbomer 940 and the emulsion (pH 6.5) is mixed at moderate speed until uniform.
  • the homogeneous o/w emulsion is then cooled to room temperature (about 25° C.) with continued moderate agitation.
  • the silicone fluid phase ingredients are added to and mixed in a suitable sized vessel equipped with mechanical dispersing means at 25° C. until a uniform solution is attained.
  • the o/w emulsion of Part 1 at 25° C. is then slowly added to the silicone fluid phase with slow mechanical stirring during addition to maintain the integrity of the double emulsion system.
  • mechanical stirring may be increased slightly in order to achieve complete uniformity and consistency of the final o/w/s multiple emulsion in lotion form.
  • the lotion emulsion of this example is rubbed on the skin in the conventional manner for applying cosmetic skin lotions, leaving the skin with a coating that moisturizes and softens the skin.
  • a moisturizing o/w/s sunscreen emulsion lotion is formed from the following ingredients (indicated by chemical or CTFA name).
  • aqueous phase ingredients other than the Carbomer 940 thickener are heated and mixed together followed by addition of the Carbomer 940 as in Example I and maintained at about 72°-75° C. with constant agitation.
  • the oil phase ingredients are mixed together in a separate vessel and maintained at about 80°-85° C.
  • the heated oil phase is then slowly added to the heated water phase, as in Example I, to form the o/w emulsion (about 70°-75° C.).
  • the emulsion After neutralization of the Carbomer 940 by addition of the triethanolamine (about 60° C.), the emulsion is further cooled with continued moderate mixing and the colorant (about 45°-50° C.) and odorant oil (about 35°-40° C.) are added, followed by cooling to room temperature (about 25° C.).
  • the four silicone fluids and other silicone phase ingredients are mixed together in a separate vessel until a uniform silicone phase is attained.
  • the o/w emulsion is slowly added to the silicone phase with stirring until a homogeneous o/w/s double emulsion in lotion form is attained.
  • the emulsion lotion leaves the skin with a coating that, in addition to providing sun-protective activity, moisturizes and softens the skin.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical & Material Sciences (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Dispersion Chemistry (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Abstract

An oil-in-water-in-silicone fluid (o/w/s) emulsion composition comprising (a) a silicone fluid continuous phase, (b) an aqueous discontinuous phase comprising an oil-in-water (o/w) emulsion, and (c) an effective dispersing amount of dimethicone copolyol for dispersing (b) in (a).

Description

This is a continuation of application Ser. No. 22,876, filed on Mar. 6, 1987, now abandoned.
BACKGROUND OF THE INVENTION
This invention relates to a multiphase (i.e., moisturizing characteristics. The multiphase emulsion composition is in the form of an oil phase/water phase/silicone fluid phase ("o/w/s multiple emulsion"). In addition to its skin moisturizing activity, the subject o/w/s multiple emulsion may be used as a base form for various products requiring an emulsified dispersion system such as cosmetic and topical drug formulations.
Single emulsion skin care preparations, such as lotions and creams, of the oil-in-water (o/w) type and water-in-oil (w/o) type are well known in the cosmetic art and are in daily use by consumers, the o/w type being more commonly utilized. Multiphase (i.e., double) emulsion compositions, such as the water-in-oil-in-water (w/o/w) type, for example see U.S. Pat. No. 4,254,105, and the oil-in-water-in oil (o/w/o) type, are of lesser commercial significance to date in the cosmetic field. In general, such single or multiphase emulsions contain water, emollients and emulsifiers as essential ingredients and cosmetically acceptable optional additives such as preservatives, antioxidants, skin conditioners, humectants, thickeners, cleansers, colorants, odorants and other components generally utilized in the cosmetic art.
To date, applicants are unaware of a skin moisturizing multiphase emulsion composition of the o/w/s type wherein "s" consists essentially of a silicone fluid. In U.S. Pat. No. 4,013,475, which represents the closest prior art known to applicants, although in an unrelated field, there is described a double emulsion wax polish for treating hard surfaces such as wood or metal. This double emulsion composition is a dispersion of an aqueous emulsion of a finely divided (0.1-5 microns) wax material in a continuous phase made up of a small amount of an organopolysiloxane of prescribed viscosity in a large volume of a hydrocarbon solvent of prescribed aniline point and distillation range characteristics (see column 6, lines 19 et seq). The particulate wax/ water emulsion is dispersed in the organopolisiloxane/hydrocarbon solvent phase by means of a non-silicone type of water-in-oil emulsifier (see column 7, lines 14 et seq). Such wax polishing emulsions, however, have obvious disadvantages for cosmetic usage. For one thing, the hydrocarbon solvent is contraindicated for skin applications due to its inherent skin-drying characteristic, indeed skin-damaging upon prolonged contact. For another, the polishing waxes are inherently water resistant and form non-permeable films, which characteristics, although suitable for application to hard surfaces such as wood or metal, are undesirable in skin care compositions. The wax polishing emulsions of U.S. Pat. 4,013,475, therefore, teach away from the skin moisturizing o/w/s multiple emulsion compositions of the subject invention which form non-occlusive, air- and moisture-permeable films upon application to the skin.
DESCRIPTION OF THE INVENTION
It has now been found that a skin moisturizing multiphase emulsion composition may be provided wherein the continuous phase consists essentially of a silicone fluid component and, in addition, an effective dispersing amount of a particular silicone fluid, namely, dimethicone copolyol, is used to disperse in said continuous phase an oil-in-water (o/w) emulsion as the aqueous discontinuous phase, the oil phase of said o/w emulsion being a liquid non-particulate containing material.
More particularly, the subject invention provides an oil-in-water-in silicone fluid (o/w/s) emulsion composition comprising three essential components, namely, a silicone fluid component as the continuous phase, an oil-in-water (o/w) emulsion as the discontinuous phase, and dimethicone copolyol as the dispersing agent, said three components being present in the indicated approximate relative percent by weight proportions:
______________________________________                                    
Component             % w/w                                               
______________________________________                                    
Silicone fluid continuous phase                                           
                      15-70                                               
o/w Emulsion discontinuous phase                                          
                      30-80                                               
Dimethicone copolyol dispersant                                           
                      0.5-5                                               
______________________________________                                    
The silicone fluid continuous phase in the subject multiphase emulsion composition consists essentially of at least one liquid organopolysiloxane such as, for example, a volatile silicone fluid, for example, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, dodecamethylcyclohexasiloxane, hexamethyldisiloxane and the like, and a non-volatile silicone fluid such as, for example, dimethicone copolyol, dimethylpolysiloxane, diethylpolysiloxane, mixed C1 -C3 alkyl (e.g., methylethyl) polysiloxane, phenyl dimethicone and high molecular weight dimethicones (average molecular weight from about 200,000 to about 1,000,000 and, preferably, from about 300,000 to about 600,000) which may have various end-terminating groups such as hydroxy, lower C1-3 alkyl, lower C1 -C3 alkoxy and the like. In accordance with a preferred embodiment, the silicone fluid continuous phase consists essentially of one or more volatile silicone fluids, preferably cyclomethicone, in admixture with one or more non- volatile silicone fluids in a respective weight ratio (volatile : non-volatile) of from about 5:1 to about 25:1 and, most preferably, from about 10:1 to about 20:1. The term "volatile" is meant to include liquid lower molecular weight organopolysiloxanes having a viscosity of from about 0.65 to about 5 centistokes at 25° C.; and "nonvolatile" meaning higher molecular weight liquid organopolysiloxanes having a viscosity higher than 5.
Liquid organopolysiloxane, also known as silicone fluids, are well known and available from various commercial suppliers. For example, several such silicone fluids are distributed by the Dow Corning Corporation, Midland, Mich., under the following designations: DC 344 Fluid, the volatile cyclomethicone; DC 3225C Fluid, a 90:10 w/w mixture of cyclomethicone and dimethicone copolyol; DC X2-1401 Fluid, a 13:87 w/w mixture of dimethiconol (hydroxy- terminated dimethicone) and cyclomethicone; and DC 556 Fluid, the non-volatile phenyl dimethicone; by The General Electric Company, Silicone Products Division, Waterford, N.Y., under its "SF" designation, for example, SF-96 for dimethicone; and SF-1173 for cyclomethicone; and by Union Carbide Corporation under its "Silicone L" series, for example, Silicone L-45 for dimethicone; and Silicone L-720 for dimethicone copolyol.
The silicone fluid continuous phase is employed in amounts ranging from about 15 to about 70 percent and, preferably, from about 18 to about 40 percent, by weight of the subject o/w/s multiple emulsion. When dimethicone copolyol constitutes the major or total part of the silicone fluid continuous phase, it also acts as the dispersing agent for the o/w emulsion discontinuous phase.
The discontinuous phase in the subject o/w/s multiple emulsion composition comprises an oil-in-water emulsion of a cosmetically acceptable oily liquid phase dispersed in an aqueous phase, generally with a pH range of about 4-8. The o/w emulsion contains from about 70 to about 99 percent and, preferably, from about 85 to about 95 percent, by weight of an aqueous continuous phase, from about 0.5 to about 25 percent and, preferably, from about 2 to about 18 percent, by weight of an oil discontinuous phase, and from about 0.5 to about 5 percent and, preferably, from about 1 to about 2 percent, by weight of a suitable oil-in-water emulsifier.
The aqueous continuous phase of the o/w emulsion may be simply water or water containing one or more soluble or dispersible cosmetically acceptable ingredients. Typical such ingredients include, for example, an emulsifier with a hyprophile-lipophile balance (HLB) value from about 12 to about 20 or even higher such as sodium alkyl polyether sulfonate, polysorbate 20, polysorbate 80, polyoxyethylene 23 lauryl ether, oleth-20 and the like; a humectant such as glycerin, polyethylene glycol, pantethine and the like; a thickener such as an acrylic acid polymer denoted by the Cosmetic, Toiletry & Fragrance Association (CTFA) name "Carbomer", a natural or synthetic gum, a cellulosic derivative and the like; a preservative or antioxidant such as methyl or propyl paraben, butylated hydroxytoluene, butylated hydroxyanisole and the like; and other water soluble additives such as a water soluble sunscreening agent, e.g., ethyl dihydroxypropyl PABA, a water soluble vitamin, e.g., vitamin C, a water soluble colorant, an electrolyte, and the like. In general, the aqueous continuous phase may contain from about 0.5 to about 15 percent by weight of such optional additives.
The oil discontinuous phase of the o/w emulsion may be simply a cosmetically acceptable oil or such oil containing one or more soluble or miscible additives generally used in cosmetic compositions. Typical such oils, also known as emollients, include mineral oil (heavy preferred), squalane, a vegetable oil such as sesame oil, safflower oil, castor oil, avocado oil and the like liquid non-wax oils. Typical oil-soluble or oil-miscible additives include, for example, a fatty (C12 -C18 preferred) acid, alcohol or ester such as myristic acid, palmitic acid, lauric acid, stearic acid, cetyl alcohol, stearyl alcohol, cetyl palmitate, octyl hydroxystearate and the like, a sterol such as cholesterol and other sterol derivatives; and a natural or synthetic wax such as beeswax, spermacetti and the like; skin penetration enhancers such as C8 -C10 triglycerides; and such other additives as oil soluble vitamins, antioxidants, preservatives, auxilliary emulsifiers and the like. The oil discontinuous phase, which may contain from about 0.5 to about 10 percent by weight of such optional additives, is prepared such that it is void of particulate matter. For example, with the optional wax additive, very small amounts are utilized in relation to the higher amount of solubilizing oil so that no particulate wax material is present in the oil phase. A particularly preferred embodiment of the oil phase comprises heavy mineral oil (0.885-0.895 specific gravity at 25° C.), cholesterol and cetyl palmitate in a respective weight ratio of about 10:5:1.
The oil-in-water emulsion is readily prepared by first thoroughly combining all the water-phase components and all the oil-phase components, including the essential emulsifying agent or agents, in separate vessels at elevated temperatures of about 60°-90° C. In general, the heated oil phase is then slowly added to the heated water phase using moderate to high speed mechanical dispersing means until a uniform o/w emulsion is obtained.
In making the oil-in-water emulsion, it is of an appropriate emulsifier which may be in the water and/or oil phase. It is of course understood that blends of emulsifiers of varying HLB values can be used to obtain the desired HLB value as determinable in the manner described in "The Atlas HLB System" (4th printing) copyright 1963 by Atlas Chemical Industries, Inc., Wilmington, Del. The emulsifier should have a hydrophile-lipophile balance such that the oil component is dispersed in the aqueous medium, generally an HLB value of not more than 14 and, preferably, from about 4 to about 12. Typical emulsifiers are such nonionic and anionic surfactants as polyoxyethylene 20 sorbitan trioleate (Polysorbate 85), sorbitan monolaurate, polyoxyethylene 4 lauryl ether sodium stearate and the like.
The multiphase oil-in-water-in-silicone fluid (o/w/s) emulsion compositions of this invention are readily prepared by using art-recognized principles and methodologies in mixing the ingredients together and in choosing the type of mixing or dispersing equipment to be used. The following Examples provide a general listing of both essential and optional components and illustrate procedures for making the subject compositions.
In general, an effective dispersing amount of dimethicone copolyol is dissolved in the silicone fluid component and then the separately prepared oil-in-water emulsion is added and dispersed, for example, by mechanical dispersing means, into the silicone fluid phase at room temperature to obtain a homogeneous dispersion of the o/w emulsion therein. The dimethicone copolyol dispersant maintains the o/w emulsion as the dispersed phase, also known as the discontinuous phase, in the silicone fluid continuous phase. Stable o/w/s emulsions having various dispersed phase volumes are easily and consistently prepared with high reproducibility. From about 0.5 to about 5 percent and, preferably, from about 1 to about 3 percent, by weight of the dimethicone copolyol dispersant may be advantageously utilized. As noted previously, dimethicone copolyol may also constitute all or part of the silicone fluid continuous phase component of the o/w/s multiple emulsion composition and may act both as the silicone fluid and the dispersant essential components of this invention. By varying the percentage of the essential components, the amounts and types of optional additives, and the shearing effect obtained from the mixing speed and time, the o/w/s multiple emulsion can be obtained in varying viscosity ranges from lotion to heavy cream form.
The subject o/w/s multiple emulsion is effective as a skin care cosmetic composition, in that it provides beneficial moisturizing activity when applied to human skin, particularly to skin cosmetically characterized as dry skin, chapped skin or rough skin. In addition, it is effective as a fundamental form for cosmetics such as lotions and creams which, in addition to providing said moisturizing action to the skin, may also provide other cosmetically desirable properties by incorporation of one or more skin care ingredients possessing a particular cosmetic characteristic, for example, sunscreening or sunblocking agents (a preferred embodiment), skin conditioners, cosmetic pigments and the like. As noted previously, for example, each of the oil and water phases of the o/w emulsion may contain optional cosmetic additives. Similarly, the silicone fluid component may also be utilized as a carrier of optional silicone miscible cosmetically acceptable additives. Typical of such additives are silicone treated pigments and talcs; ultraviolet (U.V.) absorbers for sunscreening or sunblocking protection such as octyl methoxycinnamate, benzophenone-3, silicone treated titanium dioxide and the like; polymeric skin conditioners such as, for example, the commercially available Dow Corning® QF1-593A Fluid, a mixture of dimethyl and trimethyl polysiloxane (Dow Corning Corporation, Midland, Mich.), solubilizers for U.V. absorbers or fragrances such as, for example, C.sub. 12-C15 alcohol benzoates; and the like. The subject o/w/s multiple emulsion may also be used as an effective carrier for various medicaments and drugs intended for topical skin application. For example, water soluble drugs may be incorporated into the aqueous phase of the o/w emulsion, oil soluble or oil miscible drugs may be incorporated into the oil phase of the o/w emulsion, and silicone treated or silicone miscible drugs may be incorporated into the silicone fluid component.
The following examples are intended to illustrate, but not to limit, the subject invention.
EXAMPLE I Part 1
An o/w emulsion is prepared from the following ingredients, identified by chemical or CTFA name. The indicated % w/w is based on the total weight of the finally prepared o/w/s multiple emulsion.
______________________________________                                    
Ingredient            % w/w                                               
______________________________________                                    
Aqueous Phase:                                                            
Purified water        64.85                                               
Sodium alkyl polyether sulfonate,                                         
                      1.50                                                
HLB > 12                                                                  
Carbomer 940          0.10                                                
Oil Phase:                                                                
Heavy mineral oil     1.75                                                
Cholesterol           1.00                                                
Cetyl palmitate       0.20                                                
PEG-22/Dodecyl glycol copolymer                                           
                      0.50                                                
Neutralizer Base:                                                         
Triethanolamine       0.10                                                
                      70.00                                               
______________________________________                                    
In a suitably sized vessel equipped with a suitable mechanical stirrer, (Tekmar Model RW-20 stirring motor, manufactured by IKA-WERK, Germany), the water and sulfonate emulsifier are heated to about 72°-75° C. and mixed. Stirring is increased until a vortex forms in the aqueous solution. The thickener, Carbomer 940, is slowly added to the vortex and allowed to mix until completely hydrated and the resultant gel solution is free of gelatinous particles and is uniform in composition. The temperature is maintained at about 72°-75° C. with constant agitation.
The oil phase ingredients are added to a separate suitably sized vessel and heated to about 80°-85° C. using slow mechanical stirring once the oil phase becomes molten. When molten, agitation is maintained to keep the oil phase unform during heating.
The heated oil phase is then slowly added to the heated water phase with stirring to form the o/w emulsion. After addition is complete, the mechanical dispersing means is slowed to avoid unnecessary aeration of the emulsion and mixing is continued for approximately fifteen minutes at 70°-75° C. The emulsion is then cooled to about 60° C. with moderate agitation. The base, triethanolamine, is then slowly added to neutralize the acidic Carbomer 940 and the emulsion (pH 6.5) is mixed at moderate speed until uniform. The homogeneous o/w emulsion is then cooled to room temperature (about 25° C.) with continued moderate agitation.
______________________________________                                    
Part 2:                                                                   
Ingredient         % w/w                                                  
______________________________________                                    
Silicone fluid phase:                                                     
Cyclomethicone     15.00                                                  
Dimethicone Copolyol in                                                   
                   15.00                                                  
Cyclomethicone (10:90)                                                    
                   30.00                                                  
______________________________________                                    
The silicone fluid phase ingredients are added to and mixed in a suitable sized vessel equipped with mechanical dispersing means at 25° C. until a uniform solution is attained. The o/w emulsion of Part 1 at 25° C. is then slowly added to the silicone fluid phase with slow mechanical stirring during addition to maintain the integrity of the double emulsion system. When addition is complete, mechanical stirring may be increased slightly in order to achieve complete uniformity and consistency of the final o/w/s multiple emulsion in lotion form.
The lotion emulsion of this example is rubbed on the skin in the conventional manner for applying cosmetic skin lotions, leaving the skin with a coating that moisturizes and softens the skin.
EXAMPLE II
In this example, a moisturizing o/w/s sunscreen emulsion lotion is formed from the following ingredients (indicated by chemical or CTFA name).
______________________________________                                    
Ingredient               % w/w                                            
______________________________________                                    
Aqueous Phase:                                                            
Purified water           61.17                                            
Pantethine, 80% aq. soln. (humectant)                                     
                         0.10                                             
Methylparaben (preservative)                                              
                         0.20                                             
Carbomer 940 (thickener) 0.10                                             
Glycerin (humectant)     2.50                                             
Sodium alkyl polyether sulfonate                                          
                         1.25                                             
(anionic emulsifier)                                                      
Oil Phase:                                                                
Heavy mineral oil        1.75                                             
Cholesterol (emollient & aux. emuls.)                                     
                         1.00                                             
Cetyl palmitate (aux. emuls.)                                             
                         0.20                                             
PEG-22/Dodecyl glycol copolymer (emuls.)                                  
                         0.20                                             
Ethylparaben (preservative)                                               
                         0.10                                             
Propylparaben (preservative)                                              
                         0.15                                             
Neutralizer Base:                                                         
Triethanolamine          0.10                                             
Color & Fragrance:                                                        
FD&C Red No. 4 (1% aq. soln.)                                             
                         0.03                                             
Odorant oil              0.30                                             
Silicone Phase:                                                           
Cyclomethicone/Dimethicone copolyol                                       
                         9.50                                             
(90:10)                                                                   
Cyclomethicone/Dimethiconol (13:87)                                       
                         5.00                                             
Cyclomethicone           3.00                                             
Phenyl Dimethicone       1.00                                             
Pareth-15-3 (aux. emuls.)                                                 
                         2.00                                             
Octyl Methoxycinnamate (U.V.-absorber)                                    
                         7.00                                             
Benzophenone-3 (U.V.-absorber)                                            
                         0.50                                             
C.sub.12-15 Alcohols Benzoate (solubilizer)                               
                         2.85                                             
                         100.00                                           
______________________________________                                    
The aqueous phase ingredients other than the Carbomer 940 thickener are heated and mixed together followed by addition of the Carbomer 940 as in Example I and maintained at about 72°-75° C. with constant agitation. The oil phase ingredients are mixed together in a separate vessel and maintained at about 80°-85° C. The heated oil phase is then slowly added to the heated water phase, as in Example I, to form the o/w emulsion (about 70°-75° C.). After neutralization of the Carbomer 940 by addition of the triethanolamine (about 60° C.), the emulsion is further cooled with continued moderate mixing and the colorant (about 45°-50° C.) and odorant oil (about 35°-40° C.) are added, followed by cooling to room temperature (about 25° C.).
The four silicone fluids and other silicone phase ingredients are mixed together in a separate vessel until a uniform silicone phase is attained. The o/w emulsion is slowly added to the silicone phase with stirring until a homogeneous o/w/s double emulsion in lotion form is attained.
Upon conventional application to skin areas, the emulsion lotion leaves the skin with a coating that, in addition to providing sun-protective activity, moisturizes and softens the skin.

Claims (6)

We claim:
1. An oil-in-water-in-silicon fluid emulsion composition comprising (a) from about 15% to about 70% weight of a silicone fluid continuous phase consisting essentially of at least one liquid organopolysiloxane; (b) from about 30% to about 80% by weight of an aqueous discontinuous phase comprising an oil-in-water emulsion of a cosmetically acceptable oily liquid non-particulate phase dispersed in an aqueous phase; and (c) from about 0.5% to about 5% by weight of an effective dispersing amount of dimethicone copolyol for dispersing (b) in (a).
2. The composition of claim 1 wherein said liquid organopolysiloxane is a volatile organopolysiloxane selected from the group consisting of octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, dodecamethylcyclohexasiloxane and hexamethyldisiloxane.
3. The composition of claim 1 wherein said liquid organopolysiloxane is a non-volatile organopolysiloxane selected from the group consisting of dimethylpolysiloxane, diethylpolysiloxane, mixed C1 -C3 alkyl polysiloxane, phenyl dimethicone, dimethiconol and a high molecular weight dimethicone having an average molecular weight of from about 200,000 to about 1,000,000.
4. The composition of claim 1 wherein said silicone fluid continuous phase consists essentially of one or more volatile organopolysiloxanes in admixture with one or more non-volatile organopolysiloxanes in a respective weight ratio of from about 5:1 to about 25:1.
5. The composition of claim 4 wherein said volatile organopolysiloxane is cyclomethicone.
6. The composition of claim 1 wherein the oily liquid phase of (b) comprises heavy mineral oil, cholesterol and cetyl palmitate in a respective weight ratio of about 10:5:1.
US07/312,347 1987-03-06 1989-02-15 Oil-in-water-in-silicone emulsion compositions Expired - Lifetime US4960764A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US07/312,347 US4960764A (en) 1987-03-06 1989-02-15 Oil-in-water-in-silicone emulsion compositions

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US2287687A 1987-03-06 1987-03-06
US07/312,347 US4960764A (en) 1987-03-06 1989-02-15 Oil-in-water-in-silicone emulsion compositions

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US2287687A Continuation 1987-03-06 1987-03-06

Publications (1)

Publication Number Publication Date
US4960764A true US4960764A (en) 1990-10-02

Family

ID=26696463

Family Applications (1)

Application Number Title Priority Date Filing Date
US07/312,347 Expired - Lifetime US4960764A (en) 1987-03-06 1989-02-15 Oil-in-water-in-silicone emulsion compositions

Country Status (1)

Country Link
US (1) US4960764A (en)

Cited By (134)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5183588A (en) * 1989-10-13 1993-02-02 Yves Saint Laurent Parfums Ternary system based on perfluorinated ethers
US5306498A (en) * 1991-04-05 1994-04-26 L'oreal Cosmetic composition in the form of a triple emulsion
US5380528A (en) * 1990-11-30 1995-01-10 Richardson-Vicks Inc. Silicone containing skin care compositions having improved oil control
US5420118A (en) * 1990-11-30 1995-05-30 Richardson-Vicks Inc. Gel type cosmetic compositions
US5554379A (en) * 1994-06-20 1996-09-10 Kv Pharmaceutical Company Long acting GI and esophageal protectant
US5554380A (en) * 1994-08-04 1996-09-10 Kv Pharmaceutical Company Bioadhesive pharmaceutical delivery system
EP0734718A2 (en) 1991-08-30 1996-10-02 The Procter & Gamble Company Use of N-acetyl-L-cysteine and derivatives for regulating skin wrinkles and/or skin atrophy
US5567426A (en) * 1992-07-09 1996-10-22 L'oreal Cosmetic compositon in the form of a gelled triple water/silicone oil/water emulsion
EP0689419B1 (en) * 1993-03-16 1996-12-11 L'oreal Cosmetic or topical use of an aqueous dispersion based on non-volatile organopolysiloxanes and an acrylamide or homopolymeric copolymer type cross-linked methacryloyloxyethyl trimethylammonium chloride polymer
US5670163A (en) * 1994-06-20 1997-09-23 Kv Pharmaceuticals Company Long acting GI and esophageal protectant
US5674508A (en) * 1994-07-15 1997-10-07 Laboratoires De Biologie Vegetale Yves Rocher Cosmetic composition for composing sticks for the lips or the skin and processes for the preparation thereof
US5691380A (en) * 1995-06-29 1997-11-25 The Procter & Gamble Company Stable n-acetylcysteine compositions and methods for treating human skin therewith
US5759524A (en) * 1996-02-09 1998-06-02 The Procter & Gamble Company Photoprotective compositions
US5798108A (en) * 1992-07-17 1998-08-25 L'oreal Cosmetic composition in the form of a water/oil/water triple emulsion with gelled external phase
US5834004A (en) * 1994-03-18 1998-11-10 Upmeyer; Hans-Juergen Enteral composition comprising dimethicone and a photosensitizer and a method of delivery
US5851539A (en) * 1992-10-21 1998-12-22 L'oreal Fluorocarbon continuous phase water-in-oil emulsions employing silicone surfactants
US5922335A (en) * 1995-05-15 1999-07-13 Avon Products, Inc. Uses for ascorbyl-phosphoryl-cholesterol in topical compositions
US5948416A (en) * 1995-06-29 1999-09-07 The Procter & Gamble Company Stable topical compositions
US6020367A (en) * 1997-12-02 2000-02-01 Avon Products, Inc. Supersaturated ascorbic acid solutions
US6069169A (en) * 1996-06-04 2000-05-30 Avon Products, Inc. OXA acids and related compounds for treating skin conditions
US6162450A (en) * 1995-05-15 2000-12-19 Avon Products, Inc. Uses of ascorbyl-phosphoryl-cholesterol and compositions for practicing same
US6165450A (en) * 1999-05-03 2000-12-26 Em Industries, Inc. Sprayable sunscreen compositions
US6242396B1 (en) * 1999-06-28 2001-06-05 L'oreal Cosmetic composition for removing make-up from and/or for cleansing the skin, in the form of a water-in-oil emulsion
US6242491B1 (en) 1999-06-25 2001-06-05 Rima Kaddurah-Daouk Use of creatine or creatine compounds for skin preservation
US6274124B1 (en) * 1999-08-20 2001-08-14 Dragoco Gerberding & Co. Ag Additive for improving the water resistance of cosmetic or dermatological formulations
US6290978B2 (en) 1998-04-27 2001-09-18 Larex, Inc. Derivatives of arabinogalactan and compositions including the same
US6372791B1 (en) 2000-06-29 2002-04-16 Johnson & Johnson Consumer Companies, Inc. Method of promoting skin cell metabolism
US6387382B1 (en) 1998-11-23 2002-05-14 Axiom Laboratories, Inc. Water-proof, respirable, skin barrier composition
USH2043H1 (en) 1997-05-23 2002-08-06 The Procter & Gamble Company Skin care compositions
US6432424B1 (en) 2000-06-29 2002-08-13 Johnson & Johnson Consumer Companies, Inc. Cosmetic compositions containing creatine, carnitine, and/or pyruvic acid
US20020143049A1 (en) * 2000-12-15 2002-10-03 Miller Guy Michael Compositions and methods for the prevention and treatment of cerebral ischemia
US6468552B1 (en) 2000-06-02 2002-10-22 Neutrogena Corporation Stabilized compositions containing oxygen-labile active agents
WO2002087692A1 (en) 2001-04-26 2002-11-07 The Procter & Gamble Company A method and apparatus for the treatment of cosmetic skin conditioins
WO2002092167A1 (en) * 2001-05-10 2002-11-21 The Procter & Gamble Company Method and kit for the treatment of cosmetic skin conditions
US20020182166A1 (en) * 2001-03-16 2002-12-05 Martin Katharine M. Composition containing feverfew extract and use thereof
US20020197281A1 (en) * 2001-05-21 2002-12-26 Miri Seiberg Composition cantaining a peptide and a pigment and the use thereof in darkening the skin
US20030064049A1 (en) * 2000-10-27 2003-04-03 Miri Seiberg Topical anti-cancer compositions and methods of use thereof
US6555143B2 (en) 2001-02-28 2003-04-29 Johnson & Johnson Consumer Products, Inc. Legume products
US20030138388A1 (en) * 2001-05-21 2003-07-24 Miri Seiberg Peptides and the use thereof in darkening the skin
US6649176B1 (en) 2000-06-29 2003-11-18 Johnson & Johnson Consumer Companies, Inc. Compositions containing mineral water
US6652867B1 (en) 2000-09-25 2003-11-25 Dow Corning Corporation Compositions containing organic oil-in-water emulsions, salts, alcohols and solvents
US20030232743A1 (en) * 2002-06-18 2003-12-18 Miri Seiberg Compositions and methods for darkening the skin
US20040105905A1 (en) * 1999-06-03 2004-06-03 Theresa Callaghan Method for the topical treatment and prevention of inflammatory disorders and related conditions using extracts of feverfew (Tanacetum parthenium)
US6750229B2 (en) 1998-07-06 2004-06-15 Johnson & Johnson Consumer Companies, Inc. Methods for treating skin pigmentation
US20040126351A1 (en) * 2002-12-26 2004-07-01 Avon Products, Inc. Topical composition having natural skin anti-irritant ingredient and method of use
US6797697B2 (en) 2001-05-21 2004-09-28 Johnson & Johnson Consumer Companies, Inc. Composition containing a peptide and a pigment and the use thereof in darkening the skin
US20040204333A1 (en) * 2003-03-10 2004-10-14 The Procter And Gamble Company Disposable nonwoven cleansing mitt
US20050008602A1 (en) * 2000-06-05 2005-01-13 Sumitomo Electric Industries, Ltd. Oligopeptides for promoting hair growth
US20050150784A1 (en) * 2003-03-10 2005-07-14 The Procter & Gamble Company Child's cleansing system
US20050175719A1 (en) * 2004-02-05 2005-08-11 Ying Sun Procyanidins for treatment and prevention of enzymatic irritation to the skin
US20060127431A1 (en) * 2003-03-04 2006-06-15 The Procter & Gamble Company Regulation of mammalian hair growth
US20060172904A1 (en) * 2005-01-31 2006-08-03 L'oreal Makeup-removing composition
US20060286046A1 (en) * 2005-01-05 2006-12-21 Haber C Andrew Skin care compositions
US20070004640A1 (en) * 2005-06-30 2007-01-04 Lin Connie B Treatment of dry eye
US20070020220A1 (en) * 2005-04-27 2007-01-25 Procter & Gamble Personal care compositions
US7192615B2 (en) 2001-02-28 2007-03-20 J&J Consumer Companies, Inc. Compositions containing legume products
US20070128137A1 (en) * 2005-12-02 2007-06-07 Naohisa Yoshimi Water in oil emulsion compositions containing siloxane elastomers
US7235230B2 (en) 2001-10-24 2007-06-26 Clariant Finance (Bvi) Limited Leave-on compositions for personal care
US7241731B2 (en) 2000-06-05 2007-07-10 Sumitomo Electric Industries, Ltd. Oligopeptides for promoting hair growth
US20070202061A1 (en) * 2005-10-31 2007-08-30 Naturalnano, Inc. Cosmetic skincare applications employing mineral-derived tubules for controlled release
US20070264210A1 (en) * 2006-05-15 2007-11-15 The Procter & Gamble Company Method of enhancing penetration of water-soluble actives
US20070269392A1 (en) * 2006-05-17 2007-11-22 Sunkara Hari B Personal care compositions
US20070274932A1 (en) * 2006-05-15 2007-11-29 The Procter & Gamble Company Water in oil emulsion compositions containing sunscreen actives and siloxane elastomers
US20080025917A1 (en) * 2006-04-10 2008-01-31 Malcolm Whitman Methods for modulating formation and progression of cellulite
US20080051325A1 (en) * 2003-05-16 2008-02-28 Yohei Hirai Oligopeptide
US7350256B2 (en) 2003-12-16 2008-04-01 The Procter & Gamble Company Child's aromatherapy cleaning implement
WO2008046258A1 (en) 2006-10-17 2008-04-24 Hailong Wang Cosmetic composition and preparation method and use thereof
US20080095732A1 (en) * 2005-04-27 2008-04-24 Rosemarie Osborne Personal care compositions
US7401376B2 (en) 2003-03-10 2008-07-22 The Procter & Gamble Company Disposable nonwoven cleansing mitt
US20080175875A1 (en) * 2006-09-25 2008-07-24 Hari Babu Sunkara Cosmetic compositions
US20090011035A1 (en) * 2007-07-03 2009-01-08 Joseph Michael Zukowski Personal care composition
US20090017147A1 (en) * 2005-01-14 2009-01-15 Sederma Cosmetic or Dermopharmaceutical Composition Comprising an Euglena Extract
US7490382B2 (en) 2003-12-16 2009-02-17 The Procter & Gamble Company Child's sized disposable article
US20090098173A1 (en) * 2007-10-11 2009-04-16 Robinson Ronni L Topical pain relief product
US20090105196A1 (en) * 2007-06-22 2009-04-23 Belinda Tsao Nivaggioli Use of creatine compounds to treat dermatitis
US20090123389A1 (en) * 2007-08-15 2009-05-14 Malcolm Whitman Methods for modulating Th17 cell development in the treatment and prevention of cellulite
US20090186826A1 (en) * 2003-05-12 2009-07-23 Sederma Cosmetic or dermopharmaceutical compositions of ceramides and polypeptides
US20090214607A1 (en) * 2005-05-13 2009-08-27 Sederma Topical use of teprenone
EP2105123A2 (en) 2001-03-22 2009-09-30 The Procter & Gamble Company Skin care compositions containing a sugar amine and a vitamin B3 compound
US20090253666A1 (en) * 2006-08-03 2009-10-08 Sederma Composition comprising sarsasapogenin
US20090264839A1 (en) * 2008-04-21 2009-10-22 Kriksunov Leo B Dual spray can topical delivery device
US20090269395A1 (en) * 2005-09-06 2009-10-29 Sederma Use of protoberberines as an active substance regulating the pilosebaceous unit
EP2127698A1 (en) 2001-02-28 2009-12-02 Johnson & Johnson Consumer Companies, Inc. Compositions containing legume products
US20100129301A1 (en) * 2008-11-24 2010-05-27 Shuhei Tanaka Cosmetic compositions
US20100143451A1 (en) * 2008-07-31 2010-06-10 Gruber James V Composition for Improving Skin Condition and Appearance
WO2010067327A1 (en) 2008-12-11 2010-06-17 Sederma Cosmetic composition containing acetylated oligoglucuronans
WO2010082177A2 (en) 2009-01-16 2010-07-22 Sederma New compounds, in particular peptides, compositions comprising them and cosmetic and dermopharmaceutical uses
WO2010082175A2 (en) 2009-01-16 2010-07-22 Sederma New compounds, in particular peptides, compositions comprising them and cosmetic and dermopharmaceutical uses
WO2010082176A2 (en) 2009-01-16 2010-07-22 Sederma Cosmetic composition containing kxk type peptides and uses
US20100278765A1 (en) * 2003-03-04 2010-11-04 Donald Lynn Bissett Regulation of mammalian keratinous tissue using hexamidine compositions
WO2010136965A2 (en) 2009-05-26 2010-12-02 Sederma Cosmetic use of tyr-arg dipeptide to combat cutaneous sa
US20110033507A1 (en) * 2006-02-16 2011-02-10 Sederma Polypeptides KXK and Their Use
US20110045036A1 (en) * 2006-05-05 2011-02-24 Sederma Cosmetic Compositions Comprising at Least One Peptide with at Least One Immobilized Aromatic Cycle
US7985404B1 (en) 1999-07-27 2011-07-26 Johnson & Johnson Consumer Companies, Inc. Reducing hair growth, hair follicle and hair shaft size and hair pigmentation
EP2357025A2 (en) 2009-12-17 2011-08-17 Johnson & Johnson Consumer Companies, Inc. Mild leave-on skin care compositions
US20110212100A1 (en) * 2007-08-15 2011-09-01 Tracy Keller Methods for modulating development and expansion of il-17 expressing cells
US8039026B1 (en) 1997-07-28 2011-10-18 Johnson & Johnson Consumer Companies, Inc Methods for treating skin pigmentation
US8093293B2 (en) 1998-07-06 2012-01-10 Johnson & Johnson Consumer Companies, Inc. Methods for treating skin conditions
US8106094B2 (en) 1998-07-06 2012-01-31 Johnson & Johnson Consumer Companies, Inc. Compositions and methods for treating skin conditions
WO2012130979A2 (en) 2011-03-30 2012-10-04 Lonza Inc. Topical compositions and methods for influencing electromagnetic radiation on cutaneous extracellular matrix protein production
WO2012130783A2 (en) 2011-03-27 2012-10-04 Arch Chemicals Inc. Modulating epigenetic dna methylation to cause cells to adopt dna methylation patterns associated with young cells
EP2540305A1 (en) 2011-06-28 2013-01-02 Johnson & Johnson Consumer Companies Inc. Divalent cation/talc containing compositions and methods for treating and/or preventing enzymatic irritation
EP2540291A1 (en) 2011-06-28 2013-01-02 Johnson & Johnson Consumer Companies Inc. Zinc oxide/acid containing compositions and methods for treating and/or preventing enzymatic irritation
EP2540303A1 (en) 2011-06-28 2013-01-02 Johnson & Johnson Consumer Companies Inc. Divalent cation containing compositions and methods for treating and/or preventing enzymatic irritation
US8431550B2 (en) 2000-10-27 2013-04-30 Johnson & Johnson Consumer Companies, Inc. Topical anti-cancer compositions and methods of use thereof
WO2013060771A2 (en) 2011-10-25 2013-05-02 Arch Personal Care Products, L.P. Composition containing an extract of a sequential or simultaneous fermentation
WO2013091894A2 (en) 2011-12-21 2013-06-27 Flavin Dana Topical compositions
WO2013092973A2 (en) 2011-12-22 2013-06-27 Lonza Walkersville Inc. Composition for treating skin pigmentation
WO2014052179A2 (en) 2012-09-28 2014-04-03 Johnson & Johnson Consumer Companies, Inc. Rinse-off skin care compositions containing alkyl amidopropyl betaine surfactants
WO2014074578A1 (en) 2012-11-09 2014-05-15 Johnson & Johnson Consumer Companies, Inc. Leave-on compositions containing cellulose materials
WO2014074581A1 (en) 2012-11-09 2014-05-15 Johnson & Johnson Consumer Companies, Inc. Rinse-off skin care compositions containing cellulosic materials
WO2015081007A1 (en) 2013-11-26 2015-06-04 Humco Holding Group, Inc. Transdermal silicone gel (silogel) compositions and methods of preparation
US9050477B2 (en) 2009-04-17 2015-06-09 Sederma Cosmetic compositions comprising oridonin and new cosmetic uses
US9205284B2 (en) 2010-08-09 2015-12-08 Allele Biotechnology & Pharmaceuticals, Inc. Light-absorbing compositions and methods of use
WO2016003505A1 (en) 2014-07-02 2016-01-07 Geoffrey Brooks Consultants, Llc Peptide-based compositions and methods of use
US9248088B2 (en) 2003-06-25 2016-02-02 Telomerase Activation Sciences, Inc. Compositions and methods for skin conditioning
US9284297B2 (en) 2008-08-11 2016-03-15 President And Fellows Of Harvard College Halofuginone analogs for inhibition of tRNA synthetases and uses thereof
WO2016077818A1 (en) 2014-11-14 2016-05-19 Melinta Therapeutics, Inc. Method for treating, preventing, or reducing the risk of skin infection
US9370478B2 (en) 2012-11-09 2016-06-21 Johnson & Johnson Consumer Inc. Skin care compositions containing cotton and citrus-derived materials
US9616011B2 (en) 2005-04-27 2017-04-11 The Procter & Gamble Company Personal care compositions
EP3175888A1 (en) 2015-12-02 2017-06-07 Johnson & Johnson Consumer Inc. Compositions containing polymeric sulfur and uses thereof
US9737472B2 (en) 2010-08-09 2017-08-22 Allele Biotechnology & Pharmaceuticals, Inc. Light-absorbing compositions and methods of use
US9771585B2 (en) 2015-06-05 2017-09-26 MiRagen Therapeutics, Inc. miR-155 inhibitors for treating cutaneous T cell lymphoma (CTCL)
WO2017200979A1 (en) 2016-05-17 2017-11-23 Melinta Therapeutics, Inc. Topical formulations of biaryl heterocyclic compounds and methods of use thereof
US9856290B2 (en) 2013-12-10 2018-01-02 Sussex Research Laboratories Inc. Glycopeptide compositions and uses thereof
US9993578B1 (en) 2017-01-12 2018-06-12 Lorstan Pharmaceutical, LLC Silicone oil-in-water composition useful as an injectable filler and as a scaffold for collagen growth
WO2018118874A1 (en) 2016-12-19 2018-06-28 Chromaderm, Inc. Methods of treating hyperpigmentation disorders
WO2018196993A1 (en) 2017-04-28 2018-11-01 Symrise Ag Yarrow fresh-plant pressed juice concentrate, production, and use
US10155742B2 (en) 2012-01-13 2018-12-18 President And Fellows Of Harvard College Halofuginol derivatives and their use in cosmetic and pharmaceutical compositions
US10842728B2 (en) 2010-08-09 2020-11-24 Allele Biotechnology & Pharmaceuticals, Inc. Light-absorbing compositions and methods of use
US10973748B2 (en) 2016-04-21 2021-04-13 Versitech Limited Compositions and methods for lightening skin and reducing hyperpigmentation
WO2021212076A1 (en) * 2020-04-16 2021-10-21 Baek Clinical Inc. Anhydrous urea emulsions
US11708353B2 (en) 2018-06-08 2023-07-25 The General Hospital Corporation Inhibitors of prolyl-tRNA-synthetase
US12064503B2 (en) 2020-04-16 2024-08-20 ICB (an ABC) LLC High-potency vitamin C and sugar alcohol topical formulations

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4054670A (en) * 1972-02-04 1977-10-18 Growth Products, Inc. Skin-treating composition containing polysiloxane fluids
US4254105A (en) * 1975-10-11 1981-03-03 The Lion Dentifrice Co., Ltd. Multiple emulsion having a form of water/oil/water phase and process for preparation thereof, and multiple emulsion type cosmetics
US4311695A (en) * 1979-12-03 1982-01-19 Dow Corning Corporation Personal-care emulsions comprising a siloxane-oxyalkylene copolymer
US4355046A (en) * 1980-03-19 1982-10-19 Sueess Hans R Dermatologic and cosmetic ointment base
US4370319A (en) * 1980-06-19 1983-01-25 The Procter & Gamble Company Skin conditioning compositions

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4054670A (en) * 1972-02-04 1977-10-18 Growth Products, Inc. Skin-treating composition containing polysiloxane fluids
US4254105A (en) * 1975-10-11 1981-03-03 The Lion Dentifrice Co., Ltd. Multiple emulsion having a form of water/oil/water phase and process for preparation thereof, and multiple emulsion type cosmetics
US4311695A (en) * 1979-12-03 1982-01-19 Dow Corning Corporation Personal-care emulsions comprising a siloxane-oxyalkylene copolymer
US4355046A (en) * 1980-03-19 1982-10-19 Sueess Hans R Dermatologic and cosmetic ointment base
US4370319A (en) * 1980-06-19 1983-01-25 The Procter & Gamble Company Skin conditioning compositions

Cited By (187)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5183588A (en) * 1989-10-13 1993-02-02 Yves Saint Laurent Parfums Ternary system based on perfluorinated ethers
US5380528A (en) * 1990-11-30 1995-01-10 Richardson-Vicks Inc. Silicone containing skin care compositions having improved oil control
US5420118A (en) * 1990-11-30 1995-05-30 Richardson-Vicks Inc. Gel type cosmetic compositions
US5306498A (en) * 1991-04-05 1994-04-26 L'oreal Cosmetic composition in the form of a triple emulsion
EP0734718A2 (en) 1991-08-30 1996-10-02 The Procter & Gamble Company Use of N-acetyl-L-cysteine and derivatives for regulating skin wrinkles and/or skin atrophy
US5567426A (en) * 1992-07-09 1996-10-22 L'oreal Cosmetic compositon in the form of a gelled triple water/silicone oil/water emulsion
US5798108A (en) * 1992-07-17 1998-08-25 L'oreal Cosmetic composition in the form of a water/oil/water triple emulsion with gelled external phase
US5851539A (en) * 1992-10-21 1998-12-22 L'oreal Fluorocarbon continuous phase water-in-oil emulsions employing silicone surfactants
EP0689419B1 (en) * 1993-03-16 1996-12-11 L'oreal Cosmetic or topical use of an aqueous dispersion based on non-volatile organopolysiloxanes and an acrylamide or homopolymeric copolymer type cross-linked methacryloyloxyethyl trimethylammonium chloride polymer
US5834004A (en) * 1994-03-18 1998-11-10 Upmeyer; Hans-Juergen Enteral composition comprising dimethicone and a photosensitizer and a method of delivery
US5670163A (en) * 1994-06-20 1997-09-23 Kv Pharmaceuticals Company Long acting GI and esophageal protectant
US5554379A (en) * 1994-06-20 1996-09-10 Kv Pharmaceutical Company Long acting GI and esophageal protectant
US5674508A (en) * 1994-07-15 1997-10-07 Laboratoires De Biologie Vegetale Yves Rocher Cosmetic composition for composing sticks for the lips or the skin and processes for the preparation thereof
US5554380A (en) * 1994-08-04 1996-09-10 Kv Pharmaceutical Company Bioadhesive pharmaceutical delivery system
US6162450A (en) * 1995-05-15 2000-12-19 Avon Products, Inc. Uses of ascorbyl-phosphoryl-cholesterol and compositions for practicing same
US5922335A (en) * 1995-05-15 1999-07-13 Avon Products, Inc. Uses for ascorbyl-phosphoryl-cholesterol in topical compositions
US5691380A (en) * 1995-06-29 1997-11-25 The Procter & Gamble Company Stable n-acetylcysteine compositions and methods for treating human skin therewith
US5948416A (en) * 1995-06-29 1999-09-07 The Procter & Gamble Company Stable topical compositions
US5759524A (en) * 1996-02-09 1998-06-02 The Procter & Gamble Company Photoprotective compositions
US6024942A (en) * 1996-02-09 2000-02-15 The Procter & Gamble Company Photoprotective compositions
US6069169A (en) * 1996-06-04 2000-05-30 Avon Products, Inc. OXA acids and related compounds for treating skin conditions
US6071962A (en) * 1996-06-04 2000-06-06 Avon Products, Inc. Oxa acids and related compounds for treating skin conditions
US6534543B2 (en) 1996-06-04 2003-03-18 Avon Products, Inc. Oxa acids and related compounds for treating skin conditions
US6333356B1 (en) 1996-06-04 2001-12-25 Avon Products, Inc. Compounds for treating skin conditions
USH2043H1 (en) 1997-05-23 2002-08-06 The Procter & Gamble Company Skin care compositions
US8039026B1 (en) 1997-07-28 2011-10-18 Johnson & Johnson Consumer Companies, Inc Methods for treating skin pigmentation
US6020367A (en) * 1997-12-02 2000-02-01 Avon Products, Inc. Supersaturated ascorbic acid solutions
US6290978B2 (en) 1998-04-27 2001-09-18 Larex, Inc. Derivatives of arabinogalactan and compositions including the same
US8106094B2 (en) 1998-07-06 2012-01-31 Johnson & Johnson Consumer Companies, Inc. Compositions and methods for treating skin conditions
US8093293B2 (en) 1998-07-06 2012-01-10 Johnson & Johnson Consumer Companies, Inc. Methods for treating skin conditions
US6750229B2 (en) 1998-07-06 2004-06-15 Johnson & Johnson Consumer Companies, Inc. Methods for treating skin pigmentation
US6387382B1 (en) 1998-11-23 2002-05-14 Axiom Laboratories, Inc. Water-proof, respirable, skin barrier composition
US6165450A (en) * 1999-05-03 2000-12-26 Em Industries, Inc. Sprayable sunscreen compositions
US7387807B2 (en) 1999-06-03 2008-06-17 Johnson & Johnson Consumer France, Sas, Roc Division Topical composition comprising feverfew
US7229650B2 (en) 1999-06-03 2007-06-12 Johnson & Johnson Consumer France Sas Method for the topical treatment and prevention of inflammatory disorders and related conditions using extracts of feverfew (Tanacetum parthenium)
US20050244525A1 (en) * 1999-06-03 2005-11-03 Theresa Callaghan Topical composition comprising feverfew
US20040105905A1 (en) * 1999-06-03 2004-06-03 Theresa Callaghan Method for the topical treatment and prevention of inflammatory disorders and related conditions using extracts of feverfew (Tanacetum parthenium)
US20050186195A1 (en) * 1999-06-25 2005-08-25 Avicena Group, Inc Use of creatine or creatine compounds for skin preservation
EP2397127A1 (en) 1999-06-25 2011-12-21 Enerdermics, Inc. Use of creatine or creatine compounds for skin preservation
US20050227996A1 (en) * 1999-06-25 2005-10-13 Avicena Group, Inc. Use of creatine or creatine compounds for skin preservation
US20050186194A1 (en) * 1999-06-25 2005-08-25 Avicena Group, Inc. Use of creatine or creatine compounds for skin preservation
US6242491B1 (en) 1999-06-25 2001-06-05 Rima Kaddurah-Daouk Use of creatine or creatine compounds for skin preservation
US7186754B2 (en) 1999-06-25 2007-03-06 Avicena Group, Inc. Use of creatine or creatine compounds for skin preservation
US6242396B1 (en) * 1999-06-28 2001-06-05 L'oreal Cosmetic composition for removing make-up from and/or for cleansing the skin, in the form of a water-in-oil emulsion
US7985404B1 (en) 1999-07-27 2011-07-26 Johnson & Johnson Consumer Companies, Inc. Reducing hair growth, hair follicle and hair shaft size and hair pigmentation
US6274124B1 (en) * 1999-08-20 2001-08-14 Dragoco Gerberding & Co. Ag Additive for improving the water resistance of cosmetic or dermatological formulations
US7879823B2 (en) 1999-11-05 2011-02-01 Johnson & Johnson Consumer Companies Topical anti-cancer compositions and methods of use thereof
US6468552B1 (en) 2000-06-02 2002-10-22 Neutrogena Corporation Stabilized compositions containing oxygen-labile active agents
US7241731B2 (en) 2000-06-05 2007-07-10 Sumitomo Electric Industries, Ltd. Oligopeptides for promoting hair growth
US20050008602A1 (en) * 2000-06-05 2005-01-13 Sumitomo Electric Industries, Ltd. Oligopeptides for promoting hair growth
US6649176B1 (en) 2000-06-29 2003-11-18 Johnson & Johnson Consumer Companies, Inc. Compositions containing mineral water
US6372791B1 (en) 2000-06-29 2002-04-16 Johnson & Johnson Consumer Companies, Inc. Method of promoting skin cell metabolism
US6432424B1 (en) 2000-06-29 2002-08-13 Johnson & Johnson Consumer Companies, Inc. Cosmetic compositions containing creatine, carnitine, and/or pyruvic acid
US6652867B1 (en) 2000-09-25 2003-11-25 Dow Corning Corporation Compositions containing organic oil-in-water emulsions, salts, alcohols and solvents
US7309688B2 (en) 2000-10-27 2007-12-18 Johnson & Johnson Consumer Companies Topical anti-cancer compositions and methods of use thereof
US8431550B2 (en) 2000-10-27 2013-04-30 Johnson & Johnson Consumer Companies, Inc. Topical anti-cancer compositions and methods of use thereof
US20030064049A1 (en) * 2000-10-27 2003-04-03 Miri Seiberg Topical anti-cancer compositions and methods of use thereof
US7034054B2 (en) 2000-12-15 2006-04-25 Galileo Pharmaceuticals, Inc. Methods for the prevention and treatment of cerebral ischemia using non-alpha tocopherols
US20020143049A1 (en) * 2000-12-15 2002-10-03 Miller Guy Michael Compositions and methods for the prevention and treatment of cerebral ischemia
US7192615B2 (en) 2001-02-28 2007-03-20 J&J Consumer Companies, Inc. Compositions containing legume products
EP2127698A1 (en) 2001-02-28 2009-12-02 Johnson & Johnson Consumer Companies, Inc. Compositions containing legume products
US7897144B2 (en) 2001-02-28 2011-03-01 Johnson & Johnson Comsumer Companies, Inc. Compositions containing legume products
US6555143B2 (en) 2001-02-28 2003-04-29 Johnson & Johnson Consumer Products, Inc. Legume products
US7547456B2 (en) 2001-03-16 2009-06-16 Johnson & Johnson Consumer Companies, Inc. Composition containing feverfew extract and use thereof
US20020182166A1 (en) * 2001-03-16 2002-12-05 Martin Katharine M. Composition containing feverfew extract and use thereof
EP2105123A2 (en) 2001-03-22 2009-09-30 The Procter & Gamble Company Skin care compositions containing a sugar amine and a vitamin B3 compound
US20020193831A1 (en) * 2001-04-26 2002-12-19 Smith Edward Dewey Method and apparatus for the treatment of cosmetic skin conditions
WO2002087692A1 (en) 2001-04-26 2002-11-07 The Procter & Gamble Company A method and apparatus for the treatment of cosmetic skin conditioins
WO2002092167A1 (en) * 2001-05-10 2002-11-21 The Procter & Gamble Company Method and kit for the treatment of cosmetic skin conditions
US6797697B2 (en) 2001-05-21 2004-09-28 Johnson & Johnson Consumer Companies, Inc. Composition containing a peptide and a pigment and the use thereof in darkening the skin
US7214655B2 (en) 2001-05-21 2007-05-08 Johnson & Johnson Consumer Companies, Inc. Peptides and the use thereof in darkening the skin
US20030138388A1 (en) * 2001-05-21 2003-07-24 Miri Seiberg Peptides and the use thereof in darkening the skin
US7081442B2 (en) 2001-05-21 2006-07-25 Johnson & Johnson Consumer Companies, Inc. Composition containing a peptide and a pigment and the use thereof in darkening the skin
US20020197281A1 (en) * 2001-05-21 2002-12-26 Miri Seiberg Composition cantaining a peptide and a pigment and the use thereof in darkening the skin
US7235230B2 (en) 2001-10-24 2007-06-26 Clariant Finance (Bvi) Limited Leave-on compositions for personal care
US20030232743A1 (en) * 2002-06-18 2003-12-18 Miri Seiberg Compositions and methods for darkening the skin
US7025951B2 (en) 2002-06-18 2006-04-11 Johnson & Johnson Consumer Companies, Inc. Compositions and methods for darkening the skin
US20040126351A1 (en) * 2002-12-26 2004-07-01 Avon Products, Inc. Topical composition having natural skin anti-irritant ingredient and method of use
US8591874B2 (en) 2003-03-04 2013-11-26 The Procter & Gamble Company Inhibition of mammalian hair growth
EP2997960A1 (en) 2003-03-04 2016-03-23 The Procter and Gamble Company Regulation of mammalian keratinous tissue using hexamidine compositions
US20060127431A1 (en) * 2003-03-04 2006-06-15 The Procter & Gamble Company Regulation of mammalian hair growth
US20100278765A1 (en) * 2003-03-04 2010-11-04 Donald Lynn Bissett Regulation of mammalian keratinous tissue using hexamidine compositions
US7401376B2 (en) 2003-03-10 2008-07-22 The Procter & Gamble Company Disposable nonwoven cleansing mitt
US20050150784A1 (en) * 2003-03-10 2005-07-14 The Procter & Gamble Company Child's cleansing system
US7581273B2 (en) 2003-03-10 2009-09-01 The Procter & Gamble Company Disposable nonwoven cleansing mitt
US20040204333A1 (en) * 2003-03-10 2004-10-14 The Procter And Gamble Company Disposable nonwoven cleansing mitt
US20090186826A1 (en) * 2003-05-12 2009-07-23 Sederma Cosmetic or dermopharmaceutical compositions of ceramides and polypeptides
US7560428B2 (en) 2003-05-16 2009-07-14 Sumitomo Electric Industries, Ltd. Hair growth promoting oligopeptides
US20080051325A1 (en) * 2003-05-16 2008-02-28 Yohei Hirai Oligopeptide
US9248088B2 (en) 2003-06-25 2016-02-02 Telomerase Activation Sciences, Inc. Compositions and methods for skin conditioning
US20080149504A1 (en) * 2003-12-16 2008-06-26 Joyce Marie Benjamin Child's Fragrant Cleaning Implement
US7665176B2 (en) 2003-12-16 2010-02-23 The Procter & Gamble Company Child's sized disposable article
US7490382B2 (en) 2003-12-16 2009-02-17 The Procter & Gamble Company Child's sized disposable article
US7647667B2 (en) 2003-12-16 2010-01-19 The Procter & Gamble Company Child's fragrant cleaning implement
US7350256B2 (en) 2003-12-16 2008-04-01 The Procter & Gamble Company Child's aromatherapy cleaning implement
US20050175719A1 (en) * 2004-02-05 2005-08-11 Ying Sun Procyanidins for treatment and prevention of enzymatic irritation to the skin
US20060286046A1 (en) * 2005-01-05 2006-12-21 Haber C Andrew Skin care compositions
US20090017147A1 (en) * 2005-01-14 2009-01-15 Sederma Cosmetic or Dermopharmaceutical Composition Comprising an Euglena Extract
US8741357B2 (en) 2005-01-14 2014-06-03 Sederma Sas Cosmetic or dermopharmaceutical composition comprising an euglena extract
US20060172904A1 (en) * 2005-01-31 2006-08-03 L'oreal Makeup-removing composition
US20070020220A1 (en) * 2005-04-27 2007-01-25 Procter & Gamble Personal care compositions
US10130577B2 (en) 2005-04-27 2018-11-20 The Procter & Gamble Company Personal care compositions
US9616011B2 (en) 2005-04-27 2017-04-11 The Procter & Gamble Company Personal care compositions
US20080095732A1 (en) * 2005-04-27 2008-04-24 Rosemarie Osborne Personal care compositions
US8871717B2 (en) 2005-04-27 2014-10-28 The Procter & Gamble Company Personal care compositions
US20090214607A1 (en) * 2005-05-13 2009-08-27 Sederma Topical use of teprenone
US20070004640A1 (en) * 2005-06-30 2007-01-04 Lin Connie B Treatment of dry eye
US7381707B2 (en) 2005-06-30 2008-06-03 Johnson & Johnson Consumer Companies, Inc. Treatment of dry eye
US20090269395A1 (en) * 2005-09-06 2009-10-29 Sederma Use of protoberberines as an active substance regulating the pilosebaceous unit
US8846019B2 (en) 2005-09-06 2014-09-30 Sederma Use of protoberberines as an active substance regulating the pilosebaceous unit
US20070202061A1 (en) * 2005-10-31 2007-08-30 Naturalnano, Inc. Cosmetic skincare applications employing mineral-derived tubules for controlled release
US20070128137A1 (en) * 2005-12-02 2007-06-07 Naohisa Yoshimi Water in oil emulsion compositions containing siloxane elastomers
US8404648B2 (en) 2006-02-16 2013-03-26 Sederma Polypeptides KXK and their use
US20110033507A1 (en) * 2006-02-16 2011-02-10 Sederma Polypeptides KXK and Their Use
US20080025917A1 (en) * 2006-04-10 2008-01-31 Malcolm Whitman Methods for modulating formation and progression of cellulite
US8507649B2 (en) 2006-05-05 2013-08-13 Sederma Cosmetic compositions comprising at least one peptide with at least one immobilized aromatic cycle
EP2510982A1 (en) 2006-05-05 2012-10-17 Sederma Cosmetic compositions comprising at least one peptide with at least one immobilized aromatic cycle
US20110045036A1 (en) * 2006-05-05 2011-02-24 Sederma Cosmetic Compositions Comprising at Least One Peptide with at Least One Immobilized Aromatic Cycle
US20070264210A1 (en) * 2006-05-15 2007-11-15 The Procter & Gamble Company Method of enhancing penetration of water-soluble actives
US20070274932A1 (en) * 2006-05-15 2007-11-29 The Procter & Gamble Company Water in oil emulsion compositions containing sunscreen actives and siloxane elastomers
US20090169500A1 (en) * 2006-05-17 2009-07-02 E. I. Du Pont De Nemours And Company Personal care compositions
US8029812B2 (en) 2006-05-17 2011-10-04 E. I. Du Pont De Nemours And Company Personal care compositions
US7628999B2 (en) 2006-05-17 2009-12-08 Hari Babu Sunkara Personal care compositions
US20070269392A1 (en) * 2006-05-17 2007-11-22 Sunkara Hari B Personal care compositions
US20090253666A1 (en) * 2006-08-03 2009-10-08 Sederma Composition comprising sarsasapogenin
US8361516B2 (en) 2006-08-03 2013-01-29 Sederma Composition comprising sarsasapogenin
US20080175875A1 (en) * 2006-09-25 2008-07-24 Hari Babu Sunkara Cosmetic compositions
WO2008046258A1 (en) 2006-10-17 2008-04-24 Hailong Wang Cosmetic composition and preparation method and use thereof
US20090105196A1 (en) * 2007-06-22 2009-04-23 Belinda Tsao Nivaggioli Use of creatine compounds to treat dermatitis
US20090011035A1 (en) * 2007-07-03 2009-01-08 Joseph Michael Zukowski Personal care composition
US20110212100A1 (en) * 2007-08-15 2011-09-01 Tracy Keller Methods for modulating development and expansion of il-17 expressing cells
US20090123389A1 (en) * 2007-08-15 2009-05-14 Malcolm Whitman Methods for modulating Th17 cell development in the treatment and prevention of cellulite
US20090098173A1 (en) * 2007-10-11 2009-04-16 Robinson Ronni L Topical pain relief product
US8298198B2 (en) 2008-04-21 2012-10-30 Mcneil-Ppc, Inc. Dual spray can topical delivery device
US20090264839A1 (en) * 2008-04-21 2009-10-22 Kriksunov Leo B Dual spray can topical delivery device
US9000033B2 (en) 2008-07-31 2015-04-07 Arch Personal Care Products, L.P. Composition for improving skin condition and appearance
US20100143451A1 (en) * 2008-07-31 2010-06-10 Gruber James V Composition for Improving Skin Condition and Appearance
US9284297B2 (en) 2008-08-11 2016-03-15 President And Fellows Of Harvard College Halofuginone analogs for inhibition of tRNA synthetases and uses thereof
US20100129301A1 (en) * 2008-11-24 2010-05-27 Shuhei Tanaka Cosmetic compositions
WO2010067327A1 (en) 2008-12-11 2010-06-17 Sederma Cosmetic composition containing acetylated oligoglucuronans
WO2010082176A2 (en) 2009-01-16 2010-07-22 Sederma Cosmetic composition containing kxk type peptides and uses
WO2010082175A2 (en) 2009-01-16 2010-07-22 Sederma New compounds, in particular peptides, compositions comprising them and cosmetic and dermopharmaceutical uses
WO2010082177A2 (en) 2009-01-16 2010-07-22 Sederma New compounds, in particular peptides, compositions comprising them and cosmetic and dermopharmaceutical uses
US8697656B2 (en) 2009-01-16 2014-04-15 Sederma Compounds, in particular peptides, compositions comprising them and cosmetic and dermo-pharmaceutical uses
EP3744729A1 (en) 2009-01-16 2020-12-02 Sederma Compounds, in particular peptides, compositions comprising them and cosmetic and dermopharmaceutical uses
US9050477B2 (en) 2009-04-17 2015-06-09 Sederma Cosmetic compositions comprising oridonin and new cosmetic uses
WO2010136965A2 (en) 2009-05-26 2010-12-02 Sederma Cosmetic use of tyr-arg dipeptide to combat cutaneous sa
EP2357025A2 (en) 2009-12-17 2011-08-17 Johnson & Johnson Consumer Companies, Inc. Mild leave-on skin care compositions
US9737472B2 (en) 2010-08-09 2017-08-22 Allele Biotechnology & Pharmaceuticals, Inc. Light-absorbing compositions and methods of use
US10842728B2 (en) 2010-08-09 2020-11-24 Allele Biotechnology & Pharmaceuticals, Inc. Light-absorbing compositions and methods of use
US9205284B2 (en) 2010-08-09 2015-12-08 Allele Biotechnology & Pharmaceuticals, Inc. Light-absorbing compositions and methods of use
WO2012130783A2 (en) 2011-03-27 2012-10-04 Arch Chemicals Inc. Modulating epigenetic dna methylation to cause cells to adopt dna methylation patterns associated with young cells
WO2012130979A2 (en) 2011-03-30 2012-10-04 Lonza Inc. Topical compositions and methods for influencing electromagnetic radiation on cutaneous extracellular matrix protein production
EP2540291A1 (en) 2011-06-28 2013-01-02 Johnson & Johnson Consumer Companies Inc. Zinc oxide/acid containing compositions and methods for treating and/or preventing enzymatic irritation
EP2540305A1 (en) 2011-06-28 2013-01-02 Johnson & Johnson Consumer Companies Inc. Divalent cation/talc containing compositions and methods for treating and/or preventing enzymatic irritation
EP2540303A1 (en) 2011-06-28 2013-01-02 Johnson & Johnson Consumer Companies Inc. Divalent cation containing compositions and methods for treating and/or preventing enzymatic irritation
WO2013060771A2 (en) 2011-10-25 2013-05-02 Arch Personal Care Products, L.P. Composition containing an extract of a sequential or simultaneous fermentation
WO2013091894A2 (en) 2011-12-21 2013-06-27 Flavin Dana Topical compositions
WO2013092973A2 (en) 2011-12-22 2013-06-27 Lonza Walkersville Inc. Composition for treating skin pigmentation
US10155742B2 (en) 2012-01-13 2018-12-18 President And Fellows Of Harvard College Halofuginol derivatives and their use in cosmetic and pharmaceutical compositions
WO2014052179A2 (en) 2012-09-28 2014-04-03 Johnson & Johnson Consumer Companies, Inc. Rinse-off skin care compositions containing alkyl amidopropyl betaine surfactants
US9370478B2 (en) 2012-11-09 2016-06-21 Johnson & Johnson Consumer Inc. Skin care compositions containing cotton and citrus-derived materials
US9549890B2 (en) 2012-11-09 2017-01-24 Johnson & Johnson Consumer Inc. Rinse-off skin care compositions containing cellulosic materials
US9364416B2 (en) 2012-11-09 2016-06-14 Johnson & Johnson Consumer Inc. Leave-on compositions containing cellulose materials
WO2014074578A1 (en) 2012-11-09 2014-05-15 Johnson & Johnson Consumer Companies, Inc. Leave-on compositions containing cellulose materials
US9737473B2 (en) 2012-11-09 2017-08-22 Johnson & Johnson Consumer Inc. Leave-on compositions containing cellulose materials
WO2014074581A1 (en) 2012-11-09 2014-05-15 Johnson & Johnson Consumer Companies, Inc. Rinse-off skin care compositions containing cellulosic materials
US9549889B2 (en) 2012-11-09 2017-01-24 Johnson & Johnson Consumer Inc. Rinse-off skin care compositions containing cellulosic materials
US9750689B2 (en) 2013-11-26 2017-09-05 Humco Holding Group, Inc. Transdermal silicone gel (silogel) compositions and methods of preparation
WO2015081007A1 (en) 2013-11-26 2015-06-04 Humco Holding Group, Inc. Transdermal silicone gel (silogel) compositions and methods of preparation
US9856290B2 (en) 2013-12-10 2018-01-02 Sussex Research Laboratories Inc. Glycopeptide compositions and uses thereof
WO2016003505A1 (en) 2014-07-02 2016-01-07 Geoffrey Brooks Consultants, Llc Peptide-based compositions and methods of use
US10471046B2 (en) 2014-11-14 2019-11-12 Melinta Subsidary Corp. Method for treating, preventing, or reducing the risk of skin infection
WO2016077818A1 (en) 2014-11-14 2016-05-19 Melinta Therapeutics, Inc. Method for treating, preventing, or reducing the risk of skin infection
US10316318B2 (en) 2015-06-05 2019-06-11 MiRagen Therapeutics, Inc. Oligonucleotide compositions and uses thereof
US9994852B2 (en) 2015-06-05 2018-06-12 MiRagen Therapeutics, Inc. Oligonucleotide compositions and uses thereof
US9771585B2 (en) 2015-06-05 2017-09-26 MiRagen Therapeutics, Inc. miR-155 inhibitors for treating cutaneous T cell lymphoma (CTCL)
US10238685B2 (en) 2015-12-02 2019-03-26 Johnson & Johnson Consumer Inc. Compositions containing polymeric sulfur and uses thereof
EP3175888A1 (en) 2015-12-02 2017-06-07 Johnson & Johnson Consumer Inc. Compositions containing polymeric sulfur and uses thereof
US10973748B2 (en) 2016-04-21 2021-04-13 Versitech Limited Compositions and methods for lightening skin and reducing hyperpigmentation
WO2017200979A1 (en) 2016-05-17 2017-11-23 Melinta Therapeutics, Inc. Topical formulations of biaryl heterocyclic compounds and methods of use thereof
WO2018118874A1 (en) 2016-12-19 2018-06-28 Chromaderm, Inc. Methods of treating hyperpigmentation disorders
US9993578B1 (en) 2017-01-12 2018-06-12 Lorstan Pharmaceutical, LLC Silicone oil-in-water composition useful as an injectable filler and as a scaffold for collagen growth
WO2018196993A1 (en) 2017-04-28 2018-11-01 Symrise Ag Yarrow fresh-plant pressed juice concentrate, production, and use
US11708353B2 (en) 2018-06-08 2023-07-25 The General Hospital Corporation Inhibitors of prolyl-tRNA-synthetase
WO2021212076A1 (en) * 2020-04-16 2021-10-21 Baek Clinical Inc. Anhydrous urea emulsions
US12064503B2 (en) 2020-04-16 2024-08-20 ICB (an ABC) LLC High-potency vitamin C and sugar alcohol topical formulations

Similar Documents

Publication Publication Date Title
US4960764A (en) Oil-in-water-in-silicone emulsion compositions
AU624110B2 (en) Skin conditioning composition
CA1311194C (en) Oil-in-water-in-silicone emulsion compositions
US5015469A (en) Water-in-oil emulsion type cosmetics
KR101044196B1 (en) Water-in-oil emulsion cosmetic composit ion
EP0373661B1 (en) Water-in-oil type emulsion cosmetic
JP2691729B2 (en) Solid water-in-oil emulsified cosmetic
JPH02295912A (en) Cosmetic
JP2919495B2 (en) Water-in-oil emulsion cosmetics
JPH0513126B2 (en)
JPH0420407B2 (en)
JP4081403B2 (en) O / W / O emulsified cosmetic
JPH10120525A (en) W/o-type emulsion cosmetic
JP3220177B2 (en) Water-in-oil emulsion cosmetics
JP2006241038A (en) Emulsion cosmetic
JPH0552807B2 (en)
JP2686805B2 (en) Water-in-oil emulsion cosmetics
JPH06122613A (en) Emulsion cosmetic
JPH05262618A (en) Skin-care cosmetic
JPH02258710A (en) Water-in-oil type emulsified cosmetic
KR0120276B1 (en) Oil-free type oil in water emulsification composition
JP2964261B2 (en) Oil-in-water emulsion cosmetic
JP2001342109A (en) Cosmetic
JP4126248B2 (en) Water-in-oil emulsion composition
JPH02258712A (en) Water-in-oil type emulsified cosmetic

Legal Events

Date Code Title Description
AS Assignment

Owner name: RICHARDSON-VICKS INC., TEN WESTPORT ROAD, WILTON,

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNORS:FIGUEROA, RAMON JR.;HARRISON, BOBBY G.;SA NOGUEIRA, JAMES P.;REEL/FRAME:005063/0567

Effective date: 19870305

STCF Information on status: patent grant

Free format text: PATENTED CASE

CC Certificate of correction
FEPP Fee payment procedure

Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

FPAY Fee payment

Year of fee payment: 4

FPAY Fee payment

Year of fee payment: 8

FPAY Fee payment

Year of fee payment: 12

REMI Maintenance fee reminder mailed